Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 074865

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MEXILETINE HYDROCHLORIDE (MEXILETINE HYDROCHLORIDE)
150MG
Marketing Status: Discontinued

Active Ingredient: MEXILETINE HYDROCHLORIDE
Proprietary Name: MEXILETINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074865
Product Number: 001
Approval Date: Apr 13, 1998
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

MEXILETINE HYDROCHLORIDE (MEXILETINE HYDROCHLORIDE)
200MG
Marketing Status: Discontinued

Active Ingredient: MEXILETINE HYDROCHLORIDE
Proprietary Name: MEXILETINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074865
Product Number: 002
Approval Date: Apr 13, 1998
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

MEXILETINE HYDROCHLORIDE (MEXILETINE HYDROCHLORIDE)
250MG
Marketing Status: Discontinued

Active Ingredient: MEXILETINE HYDROCHLORIDE
Proprietary Name: MEXILETINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A074865
Product Number: 003
Approval Date: Apr 13, 1998
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information